反応式
[NH:1]1[CH2:6][CH2:5][CH2:4][CH:3](CC(OCC)=O)[CH2:2]1.[CH2:13]([O:15][C:16](=[O:24])[CH2:17]C1C=CC=CN=1)[CH3:14]>>[N:1]1([CH2:17][C:16]([O:15][CH2:13][CH3:14])=[O:24])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1参加物
3
実験手順
The reaction was run in the same manner as ethyl 3-piperidinylacetate, starting with commercially available ethyl-2-pyridylacetate (4.00 g; 24.5 mmol). This gave ethyl 2-piperidinylacetate (2.41 g) as a light yellow oil without further purification. MS m/z (positive ion) 172 (MH+; 100).
後処理
- customThis gave ethyl 2-piperidinylacetate (2.41 g) as a light yellow oil without further purification
出典と根拠
- ORDレコード
- ord-885d55a01d27437bb29c8817847259b2
- 出典データセット
- uspto-grants-2003_12
- 特許番号
- US06664271B1
関連ノート
読み込み中…